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基于植物表达抗体的黄曲霉毒素 M1 诊断免疫分析方法的设计。

Design of a Diagnostic Immunoassay for Aflatoxin M1 Based on a Plant-Produced Antibody.

机构信息

Laboratory Biotechnologies, Department of Sustainability, ENEA, Casaccia Research Center, Via Anguillarese 301, 00123 Rome, Italy.

Euroclone S.p.A., Via Figino 20/22, 20016 Milano, Italy.

出版信息

Toxins (Basel). 2022 Dec 3;14(12):851. doi: 10.3390/toxins14120851.

Abstract

A new green competitive ELISA for aflatoxin M1 quantification in raw milk was developed. This diagnostic tool is based on an anti AFM1 mAb produced by plant molecular farming in alternative to classical systems. Our assay, showing an IC below 25 ng/L, fits with the requirements of EU legislation limits for AFM1 (50 ng/L). Optimal accuracy was achieved in correspondence of the decision levels (25 and 50 ng/L), and the assay enabled AFM1 quantification in the range 5-110 ng/L, with limit of detection 3 ng/L. Moreover, to evaluate a real applicability in diagnostics, raw milk-spiked samples were analysed, achieving satisfactory recovery rates of AFM1. In conclusion, an efficient and ready-to-use diagnostic assay for the quantification of aflatoxin M1 in milk, based on a plant-produced recombinant mAb, has been successfully developed.

摘要

建立了一种用于检测生奶中黄曲霉毒素 M1 的新型绿色竞争 ELISA 方法。该诊断工具基于植物分子农业生产的抗 AFM1 mAb,替代了传统系统。我们的检测方法,IC 低于 25ng/L,符合欧盟法规对 AFM1(50ng/L)的限量要求。在决策水平(25 和 50ng/L)处达到最佳准确性,并且该检测方法能够在 5-110ng/L 的范围内定量 AFM1,检测限为 3ng/L。此外,为了评估在诊断中的实际应用,对生奶加标样品进行了分析,获得了令人满意的 AFM1 回收率。总之,成功开发了一种基于植物表达的重组 mAb 用于检测牛奶中黄曲霉毒素 M1 的高效、即用型诊断方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efb8/9781297/b039b789fb4f/toxins-14-00851-g001.jpg

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